The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125016182 12501618 2 F 20021201 20160610 20160627 20160802 EXP GB-APOTEX-2016AP009455 APOTEX 29.00 YR F Y 0.00000 20160802 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125016182 12501618 1 SS PAROXETINE HYDROCHLORIDE. PAROXETINE HYDROCHLORIDE 1 Unknown UNK U U 0
125016182 12501618 2 PS PAROXETINE. PAROXETINE 1 Oral 20 MG, UNK U U 75356 20 MG TABLET
125016182 12501618 3 SS PAROXETINE. PAROXETINE 1 Oral 5 MG, QD U U 75356 5 MG TABLET QD
125016182 12501618 4 SS Paroxetine Oral solution PAROXETINE 1 Oral 5 ML, QD U 0 5 ML ORAL SOLUTION QD
125016182 12501618 5 SS Paroxetine Oral solution PAROXETINE 1 Oral 7.25 ML, QD U 0 7.25 ML ORAL SOLUTION QD
125016182 12501618 6 SS Paroxetine Oral solution PAROXETINE 1 Oral 8 ML, QD U 0 8 ML ORAL SOLUTION QD
125016182 12501618 7 SS SEROXAT PAROXETINE HYDROCHLORIDE 1 Unknown UNK U 0
125016182 12501618 8 C MIRTAZAPINE. MIRTAZAPINE 1 UNK U 0
125016182 12501618 9 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 UNK U 0
125016182 12501618 10 C HYDROXYZINE HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 UNK U 0
125016182 12501618 11 C DIAZEPAM. DIAZEPAM 1 UNK U 0
125016182 12501618 12 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK U 0
125016182 12501618 13 C Stemetil PROCHLORPERAZINE MALEATE 1 UNK U 0
125016182 12501618 14 C BUSPIRONE BUSPIRONE HYDROCHLORIDE 1 UNK U 0
125016182 12501618 15 C Contraceptive pill 2 Oral UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125016182 12501618 1 Depression
125016182 12501618 4 Depression
125016182 12501618 7 Depression
125016182 12501618 8 Product used for unknown indication
125016182 12501618 9 Product used for unknown indication
125016182 12501618 10 Product used for unknown indication
125016182 12501618 11 Product used for unknown indication
125016182 12501618 12 Product used for unknown indication
125016182 12501618 13 Product used for unknown indication
125016182 12501618 14 Product used for unknown indication
125016182 12501618 15 Anxiety

Outcome of event

Event ID CASEID OUTC COD
125016182 12501618 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125016182 12501618 Abdominal pain upper
125016182 12501618 Agitation
125016182 12501618 Anxiety
125016182 12501618 Decreased appetite
125016182 12501618 Disturbance in attention
125016182 12501618 Drug withdrawal syndrome
125016182 12501618 Dysarthria
125016182 12501618 Epigastric discomfort
125016182 12501618 Fatigue
125016182 12501618 Feeding disorder
125016182 12501618 Influenza like illness
125016182 12501618 Insomnia
125016182 12501618 Loss of consciousness
125016182 12501618 Muscle tightness
125016182 12501618 Nervousness
125016182 12501618 Night sweats
125016182 12501618 Panic reaction
125016182 12501618 Paraesthesia
125016182 12501618 Sensory disturbance
125016182 12501618 Social avoidant behaviour
125016182 12501618 Tearfulness
125016182 12501618 Tremor

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125016182 12501618 1 20010109 20101223 0
125016182 12501618 2 20030509 20080111 0
125016182 12501618 3 20110901 0
125016182 12501618 4 20030613 20100802 0
125016182 12501618 5 20100823 0
125016182 12501618 6 20100917 20101221 0
125016182 12501618 7 20110719 20110727 0
125016182 12501618 8 20030509 0
125016182 12501618 9 20030613 0
125016182 12501618 11 20010102 20050722 0
125016182 12501618 12 19980121 20010109 0
125016182 12501618 13 200507 0
125016182 12501618 14 200508 0
125016182 12501618 15 200701 0